CRYSTAL FORM OF PYRIMIDINE SULFONAMIDE COMPOUND AND PREPARATION METHOD THEREFOR

Disclosed are a Crystal Form (I) of a pyrimidine sulfonamide compound and a preparation method therefor. The present disclosure relates to an application thereof in the preparation of a medicament for treating diseases related to ETA receptor antagonists.

Skip to: Description  ·  Claims  · Patent History  ·  Patent History
Description
CROSS REFERENCE TO RELATED APPLICATION

The present application claims priority to the following application:

Chinese Application No. 201910428795.9, filed on May 22, 2019.

TECHNICAL FIELD

Provided are crystal forms of a pyrimidine sulfonamide compound and preparing process thereof, as well as use of the crystal forms for the manufacture of a medicament for treating a disease related to ETA receptor antagonists.

BACKGROUND

Endothelins (ETs) are a family of isopeptides containing 21 amino acids, all with a hydrophobic C-terminus consisting of six identical amino acid residues and two intra-chain disulfide bonds. There are three different genetically encoded isoforms occurring in the human body: ET-1, ET-2 and ET-3, among which ET-1 has the strongest vasoconstrictive activity. It induces three to ten times higher vasoconstrictive strength in veins than in arteries, and is the main isoform that underlies diseases. ET-1 is the most abundant and functionally important member of the endothelin family. It is mainly expressed in the vascular endothelium but is also found in non-vascular tissues of the heart, kidney, lung, adrenal glands and other organs.

ETs function not only as vascular factors in the regulation of blood pressure, but also as hormones in many cellular processes (such as proliferation, apoptosis and migration) leading to tissue hypertrophy, remodeling, fibrosis and inflammation. Elevated plasma and tissue levels of ET-1 are seen in a variety of diseases, for example, pulmonary hypertension, hypertension, sepsis, atherosclerosis, acute myocardial infarction, congestive heart failure, migraine and asthma, etc. Therefore, endothelin receptor antagonists have been extensively studied as very promising therapeutic agents.

Endothelin receptors belong to G protein-coupled receptors. Currently, there are mainly three known endothelin receptors, ETA, ETB and ETC, which show different distribution in different tissues and organs, and have different affinities for the three endothelin isoforms, and differ significantly in their physiological effects. Endothelin ETA receptor predominantly distributes on smooth muscle cells. It selectively binds to ET-1 and mediates the contraction of vascular smooth muscle. Endothelin ETB receptors can be divided into two subtypes, ETB1 and ETB2; the former distributes in endothelial cells and mediates the release of endothelium-derived relaxing factor (EDRF), prostacyclin (PGI2) and nitric oxide (NO), causing vasodilation; and the latter are located on vascular smooth muscle and acts like ETA receptors, directly mediating venous vasoconstriction. Endothelin ETB receptors show comparable affinities for ET-1, ET-2 and ET-3. The ETC receptor is an ET-3 selective receptor that mainly distributes in neuronal cells and acts as a neurotransmitter. ET-1 acts mainly through ETA and ETB receptors. Endothelin receptor antagonists can be classified into three types: ETA receptor antagonists, ETB receptor antagonists and dual ETA/ETB antagonists. The preclinical and/or clinical effects of endothelin receptor antagonists have been demonstrated on many diseases such as subarachnoid hemorrhage, heart failure, pulmonary hypertension, essential hypertension, refractory hypertension, neurogenic inflammation, diabetic nephropathy, focal segmental glomerulosclerosis, renal failure, neurogenic inflammation, and cerebral vasospasm following renal failure and myocardial infarction. Highly selective ETA receptor antagonists inhibit the strong vasoconstrictive effects of ET-1 while avoiding some of the adverse effects of non-selective dual ETA/ETB receptor antagonists, thereby reducing clinical side effects.

Patent publication WO200205355 discloses the compound Macitentan, which can be used for the treatment of diseases associated with the effects of endothelins.

SUMMARY

Provided is a Crystal Form A of the compound as shown in formula (I), characterized in that, the Crystal Form A has an X-ray powder diffraction pattern having characteristic diffraction peaks at the following 2θ angles: 12.62±0.20°, 16.86±0.20°, 19.33±0.20°, and 25.38±0.20°.

In some embodiments of the present disclosure, the Crystal Form A has an X-ray powder diffraction pattern having characteristic diffraction peaks at the following 2θ angles: 8.42±0.20°, 10.31±0.20°, 12.62±0.20°, 16.86±0.20°, 18.28±0.20°, 19.33±0.2°, 21.87±0.20°, 25.38±0.20°, and 27.14±0.20°.

In some embodiments of the present disclosure, the Crystal Form A has an X-ray powder diffraction pattern having characteristic diffraction peaks at the following 2θ angles: 8.42±0.20°, 10.31±0.20°, 12.62±0.20°, 16.86±0.20°, 18.28±0.20°, 19.33±0.2°, 21.87±0.20°, 22.93±0.20°, 25.38±0.20°, 26.63±0.20°, and 27.14±0.20°.

In some embodiments of the present disclosure, the Crystal Form A has an X-ray powder diffraction pattern having characteristic diffraction peaks at the following 2θ angles: 8.42°, 9.41°, 9.58°, 9.82°, 10.31°, 12.62°, 15.77°, 16.62°, 16.86°, 17.51°, 17.97°, 18.28°, 18.85°, 19.33°, 19.58°, 20.33°, 21.87°, 22.58°, 22.93°, 23.15°, 23.39°, 25.05°, 25.38°, 26.31°, 26.63°, 27.14°, 27.79°, 29.40°, 31.01°, 31.48°, 35.42°, and 39.21°.

In some embodiments of the present disclosure, the Crystal Form A has an XRPD pattern as shown in FIG. 1.

In some embodiments of the present disclosure, the Crystal Form A has an XRPD pattern with analysis data as shown in Table 1.

TABLE 1 XRPD Pattern Analysis Data of Crystal Form A of the compound of formula (I) 2θ Interplanar Relative angle spacing intensity No. (°) (Å) (%) 1 8.417 10.496 10.2 2 9.406 9.3946 5.9 3 9.584 9.2203 4.4 4 9.822 8.9973 3.6 5 10.309 8.5741 8.6 6 12.623 7.0069 52.2 7 15.774 5.6136 3.4 8 16.624 5.3283 11 9 16.859 5.2547 32.4 10 17.514 5.0596 5.2 11 17.971 4.9318 5.8 12 18.278 4.8497 11.2 13 18.85 4.7039 3.4 14 19.327 4.5887 68.1 15 19.579 4.5302 4 16 20.328 4.3651 5.1 17 21.867 4.0612 14.4 18 22.579 3.9347 5.2 19 22.933 3.8748 13.4 20 23.152 3.8386 13 21 23.39 3.8001 4.6 22 25.047 3.5523 5.6 23 25.383 3.5061 100 24 26.314 3.3841 5.6 25 26.626 3.3451 12.2 26 27.135 3.2836 26.8 27 27.79 3.2076 6.1 28 29.403 3.0351 3.1 29 31.008 2.8817 6.5 30 31.475 2.8399 3.2 31 35.418 2.5323 4.8 32 39.207 2.2959 5.7

In some embodiments of the present disclosure, the Crystal Form A has a differential scanning calorimetry curve having the onset point of an endothermic peak at 161.3±3.0° C.

In some embodiments of the present disclosure, the Crystal Form A has a DSC pattern as shown in FIG. 2.

In some embodiments of the present disclosure, the Crystal Form A has a thermogravimetric analysis curve having a weight loss of 0.01% at 152.3±3.0° C.

In some embodiments of the present disclosure, the Crystal Form A has a TGA pattern as shown in FIG. 3.

Provided is a Crystal Form B of the compound as shown in formula (I), characterized in that, the Crystal Form B has an X-ray powder diffraction pattern having characteristic diffraction peaks at the following 2θ angles: 7.51±0.20°, 9.60±0.20°, and 22.56±0.20°.

Provided is a Crystal Form B of the compound as shown in formula (I), characterized in that, the Crystal Form B has an X-ray powder diffraction pattern having characteristic diffraction peaks at the following 2θ angles: 7.51±0.20°, 22.56±0.20°, and 24.79±0.20°.

Provided is a Crystal Form B of the compound as shown in formula (I), characterized in that, the Crystal Form B has an X-ray powder diffraction pattern having characteristic diffraction peaks at the following 2θ angles: 7.51±0.20°, 15.05±0.20°, 22.56±0.20°, and 24.79±0.20°.

In some embodiments of the present disclosure, the Crystal Form B has an X-ray powder diffraction pattern having characteristic diffraction peaks at the following 2θ angles: 7.51±0.20°, 9.60±0.20°, 15.05±0.20°, 19.09±0.20°, 22.56±0.20°, 24.18±0.20°, 24.79±0.20°, and 27.95±0.20°.

In some embodiments of the present disclosure, the Crystal Form B has an X-ray powder diffraction pattern having characteristic diffraction peaks at the following 2θ angles: 7.51±0.20°, 9.60±0.20°, 15.05±0.20°, 19.09±0.20°, 22.20±0.20°, 22.56±0.20°, 24.18±0.20°, 24.79±0.20°, and 27.95±0.20°.

In some embodiments of the present disclosure, the Crystal Form B has an X-ray powder diffraction pattern having characteristic diffraction peaks at the following 2θ angles: 7.51°, 9.60°, 11.08°, 15.05°, 15.52°, 17.53°, 18.34°, 19.09°, 20.41°, 20.85°, 22.20°, 22.56°, 23.15°, 24.18°, 24.79°, 27.69°, 27.95°, 28.75°, 33.57°, and 35.42°.

In some embodiments of the present disclosure, the Crystal Form B has an XRPD pattern as shown in FIG. 4.

In some embodiments of the present disclosure, the Crystal Form B has an XRPD pattern with analysis data as shown in Table 2.

TABLE 2 XRPD Pattern Analysis data of Crystal Form B of the compound of formula (I) 2Θ Interplanar Relative angle spacing intensity No. (°) (Å) (%) 1 7.513 11.7575 84.1 2 9.602 9.2036 38.3 3 11.078 7.9801 16.4 4 15.047 5.8829 60.9 5 15.515 5.7066 18.3 6 17.533 5.054 15.5 7 18.336 4.8345 23.5 8 19.088 4.6456 56.4 9 20.41 4.3476 19.4 10 20.845 4.2578 28.6 11 22.202 4.0006 60.9 12 22.562 3.9376 100 13 23.15 3.839 26.6 14 24.179 3.6778 43.1 15 24.789 3.5887 82.6 16 27.688 3.2192 20.1 17 27.946 3.1901 55.1 18 28.754 3.1022 19.8 19 33.567 2.6676 13.5 20 35.419 2.5322 16.6

In some embodiments of the present disclosure, the Crystal Form B has a differential scanning calorimetry curve having the onset point of an endothermic peak at 150.3±3.0° C.

In some embodiments of the present disclosure, the Crystal Form B has a DSC pattern as shown in FIG. 5.

In some embodiments of the present disclosure, the Crystal Form B has a thermogravimetric analysis curve having a weight loss of 0.53% at 90.0±3.0° C., and a further weight loss of 0.60% at 143.9±3.0° C.

In some embodiments of the present disclosure, the Crystal Form B has a TGA pattern as shown in FIG. 6.

In some embodiments of the present disclosure, provided is a process for preparing the Crystal Form A of the compound as shown in formula (I), comprising:

(1) adding the compound as shown in formula (I) into a solvent, with heating for dissolving;

(2) cooling the solution in (1) until a solid is precipitated; stirring; and filtering to give the Crystal Form A of the compound of formula (I).

In some embodiments of the present disclosure, in the preparation process, the solvent is selected from the group consisting of tetrahydrofuran and acetonitrile.

In some embodiments of the present disclosure, in the preparation process, the stirring is conducted at the temperature of 10° C. to 60° C.

In some embodiments of the present disclosure, in the preparation process, the stirring time is 12 hours to 24 hours.

In some embodiments of the present disclosure, in the preparation process, the weight-volume ratio of the compound to the solvent is 1 g:1-6 mL.

In some embodiments of the present disclosure, provided is a process for preparing the Crystal Form B of the compound as shown in formula (I), comprising:

(1) adding the compound as shown in formula (I) into a solvent with complete dissolution;

(2) adding amino acid; stirring at 40° C. for 12-24 hours; and filtering to give the Crystal Form B of the compound of formula (I);

wherein,

the solvent is selected from the group consisting of tetrahydrofuran;

the amino acid is selected from the group consisting of L-arginine.

Also provided is use of the crystal forms for the manufacture of a medicament for treating a disease related to ETA receptor antagonists.

In some embodiments of the present disclosure, the use is characterized in that, the ETA receptor antagonist-related medicament is a medicament for indications such as pulmonary hypertension, essential hypertension, refractory hypertension, diabetic nephropathy and intracranial vasospasm, etc.

General Definition

Unless stated otherwise, the terms and phrases used herein have the following meaning. A specific term or phrase shall not be considered as indefinite or unclear when it is not specifically defined. It should be understood according to the general meaning. The trade name used herein refers to the corresponding product or the active ingredient.

The intermediate compounds can be prepared through various synthesis processes well-known to a person skilled in the art, including the specific embodiments illustrated below, the embodiments through combination of such specific embodiments with other chemical synthesis processes as well as equivalents well-known to a person skilled in the art. The preferable embodiments comprise but not limited to the Examples herein.

The chemical reaction of the specific embodiments is performed in a suitable solvent, and the solvent should be suitable for the chemical changes of the present disclosure and the required reagents and materials. To obtain the compound of the present disclosure, a person skilled in the art can modify or select a synthesis step or a reaction scheme based on the available embodiments.

The present disclosure will be specifically described hereinafter by Examples. The Examples should be not interpreted as limitation to the present disclosure.

The solvents used herein are commercially available and can be used without further purification.

The solvents used in the present disclosure are commercially available. The following abbreviations are used: ACN for acetonitrile; DCM for dichloromethane; DMF for N,N-dimethylformamide; DMSO for dimethylsulfoxide; EtOH for ethanol; MeOH for methanol; TFA for trifluoroacetic acid; ATP for adenosine triphosphate; HEPES for 4-hydroxyethyl piperazine ethanesulfonic acid.

Technical Effect

The crystal forms of the compound of the present disclosure has good stability and promising druggability. The compounds of the present disclosure all exhibit extremely high in vitro antagonistic activity against the human ETA receptor, as well as ETA/ETB selectivity of over 10,000-fold. The compound of the present disclosure was superior to the control Macitentan in characterization experiments of PXR-mediated induction of CYP3A expression. The compound of the present disclosure was superior to Macitentan in the characterization experiments of the inhibition of all the five major isozymes of human liver microsomal cytokine P450. The compound of the present disclosure exhibits much weaker inhibitory effect on bile salt export pump than Macitentan, thereby significantly reducing the risk of producing hepatotoxicity. The compound of the present disclosure have a good in vivo pharmacokinetic profile both in SD rats and Beagle dogs.

1.1 X-Ray Powder Diffractometer (XRPD)

  • Instrument type: Bruker D8 advance X-ray diffractometer
  • Testing method: about 10-20 mg of sample is used for XRPD detection.
  • Detailed XRPD parameters are as follows:
  • Light tube: Cu, kα, (λ=1.54056 Å).
  • Light tube voltage: 40 kV, Light tube current: 40 mA
  • Divergence slit: 0.60 mm
  • Detector slit: 10.50 mm
  • Anti-scatter slit: 7.10 mm
  • Scanning range: 4-40 deg
  • Step size: 0.02 deg
  • Time/step: 0.12 s
  • Sample stage spinning speed: 15 rpm

1.2 Differential Scanning Calorimeter (DSC)

  • Instrument type: TA Q2000 Differential Scanning Calorimeter
  • Testing method: The sample (about 1 mg) is placed in DSC aluminum pot for testing, under 50 mL/min N2, with the heating rate of 10° C./min, and the sample is heated from 25° C. to 350° C.

1.3 Thermal Gravimetric Analyzer (TGA)

  • Instrument type: TA Q5000IR Thermal Gravimetric Analyzer
  • Testing method: The sample (2-5 mg) was placed in TGA platinum pot for testing, under 25 mL/min N2, with the heating rate of 10° C./min, and the sample is heated from room temperature to 350° C.

1.4 Hygroscopicity Test

  • The hygroscopicity test of Crystal Form A of the compound of formula (I) of the present disclosure is performed according to the Guidelines for Stability Testing of APIs and Formulations (Chinese Pharmacopoeia 2015 Edition, Volume IV, General Principles).
  • Categorization in the hygroscopicity evaluation is as follows:

Hygroscopicity categorization ΔW % Deliquescence Absorbs sufficient water to form a liquid Highly hygroscopic ΔW % ≥ 15% Hygroscopic 15% > ΔW % ≥ 2% Slightly hygroscopic 2% > ΔW % ≥ 0.2% Non- or almost non-hygroscopic ΔW % < 0.2% Note: ΔW % represents the percentage of moisture-absorption weight gain of the test article at 25° C. in a desiccator with a saturated solution of ammonium chloride in the lower part

1.5 High Performance Liquid Chromatographic Analytical Method

  • See Table 3 below for chromatographic conditions for the HPLC method of solid stability testing:

TABLE 3 Chromatographic column Waters Xbridge C18, 4.6 mm × 150 mm, 3.5 μm, (PN: 186003034) Wave length 220 nm Column temperature 35° C. Flow Rate 0.8 mL/min Injection temperature No temperature control Injection volume 10 μL Mobile phase A: pH 9.0 10 mmol/L ammonium acetate buffer solution B: ACN Time (minutes) A % B % Mobile phase procedure 0.0 90 10 10.0 90 10 30.0 40 60 40.0 20 80 45.0 20 80 45.1 90 10 55.0 90 10 Data acquisition time 60 minutes Diluter Acetonitrile:NaOH (V/V) = 1:1

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows the XRPD spectrum by Cu-Kα radiation of Crystal Form A of the compound of formula (I).

FIG. 2 shows the DSC spectrum of the Crystal Form A of the compound of formula (I).

FIG. 3 shows the TGA spectrum of the Crystal Form A of the compound of formula (I).

FIG. 4 shows the XRPD spectrum by Cu-Kα radiation of Crystal Form B of the compound of formula (I).

FIG. 5 shows the DSC spectrum of the Crystal Form B of the compound of formula (I).

FIG. 6 shows the TGA spectrum of the Crystal Form B of the compound of formula (I).

 EXAMPLES

The following Examples are provided for further illustration for the purpose of better understanding of the present disclosure. The specific embodiments should not be interpreted as limitation to the present disclosure.

Example 1: Preparation of the Compound of Formula (I)

Step 1: Synthesis of Compound 3

Compound 2 (1275 g, 9.01 mol) was dissolved in dichloromethane (5.5 L) at 5-10° C. under nitrogen protection. tert-Butanol (801.23 g, 10.81 mol) was slowly added dropwise at a controlled temperature of 15-20° C. to the solution (dropwise addition during about 2 hr). The reaction mixture was stirred at room temperature for 4 hours. The target compound 3 (crude) was kept in the reaction solvent dichloromethane (5.5 L) and used directly in the next step of the reaction.

Step 2: Synthesis of Compound 4

Compound 2-methoxyethylamine (676.74 g, 9.01 mol) was dissolved in dichloromethane (2.0 L) at 5-10° C. under nitrogen protection. Then triethylamine (1823.44 g, 18.02 mol) was added. The internal temperature was maintained at 10-15° C., and a solution of compound 3 in dichloromethane (9.01 mol, 5.5 L) was slowly added dropwise to the reaction solution (dropwise addition during about 2 hr). The reaction mixture was allowed to warm to room temperature and stirred for 12 hours. After the reaction was complete, 2 M dilute hydrochloric acid was added to the reaction solution to adjust the pH to 3-4. The water layer was separated and discarded. The organic phase was washed with water (2 L×2), dried over anhydrous sodium sulphate and filtered. The filtrate was concentrated under reduced pressure to give the target compound 4. 1H NMR (400 MHz, CDCl3) δ: 7.24 (br s, 1H), 5.45 (t, J=5.6 Hz, 1H), 3.53 (t, J=5.0 Hz, 2H), 3.37 (s, 3H), 3.26 (q, J=5.4 Hz, 2H), 1.51 (s, 9H).

Step 3: Synthesis of Compound 5

Compound 4 (1912.50 g, 7.52 mol) was added to water (7.0 L) at 5-10° C. The reaction mixture was heated to 90-95° C. and stirred for 4 hours. After cooling to room temperature. Extraction was performed with ethyl acetate (2.0 L×2). The aqueous phase was collected. The organic phase was combined and washed with water (2.0 L). The organic phase was separated and discarded. The two aqueous phases were combined and concentrated under reduced pressure to give the target compound 5. 1H NMR (400 MHz, CDCl3) δ: 5.38-5.35 (m, 3H), 3.54 (t, J=5.1 Hz, 2H), 3.36 (s, 3H), 3.30-3.26 (m, 2H).

Step 4: Synthesis of Compound 6

Compound 5 (609.05 g, 3.95 mol) was dissolved in dimethyl sulfoxide (5.0 L) at 5-10° C. under nitrogen protection. Then potassium tert-butoxide (1107.51 g, 9.87 mol) was added and the reaction mixture was stirred at 15-20° C. for 1 h. A solution of 5-bromo-4,6-dichloropyrimidine (750.03 g, 3.29 mol) in dimethyl sulfoxide (2.0 L) was slowly added dropwise to the reaction solution (dropwise addition during about 2 hr) and the reaction mixture was stirred for another 12 h at room temperature. Two batches of reaction were performed in parallel at the same scale, and then combined for work-up. After the reaction was complete, the reaction solution was poured into cold water (42 L). The pH was adjusted to 3-4 with 2 M dilute hydrochloric acid. Extraction was conducted with ethyl acetate (20 L×4). The organic phases were combined, washed with saline (15 L), dried over anhydrous sodium sulphate, and filtered. The solvent was removed from the filtrate under reduced pressure. The resulting crude product was slurried with methanol (1.2 L) and stirred for 30 minutes, filtered and the filter cake was washed with methanol (100 mL×2). The filter cake was collected and the solvent was remove under reduced pressure to give the target compound 6. 1H NMR (400 MHz, CDCl3) δ: 8.50 (s, 1H), 7.80 (s, 1H), 5.89 (t, J=5.6 Hz, 1H), 3.41 (t, J=5.0 Hz, 2H), 3.21-3.17 (m, 5H).

Step 5: Synthesis of Compound 7

At 5-10° C. under nitrogen protection, potassium tert-butoxide (195.25 g, 1.74 mol) was added to ethylene glycol (1.6 L). The reaction mixture was heated to 40° C. and stirred for 1 h. Then compound 6 (200.80 g, 0.58 mol) and ethylene glycol dimethyl ether (100.00 mL) were added sequentially to the solution. The reaction solution was heated to 110° C. and stirred for another 12 hours. After the reaction was complete, the reaction was cooled to room temperature, and the reaction solution was poured into ice water (6.5 L). The pH was adjusted to 3-4 with 2 M dilute hydrochloric acid. Extraction was conducted with ethyl acetate (2.5 L×4). The organic phases were combined, washed with saline (2.0 L×2), dried over anhydrous sodium sulphate, and filtered. The solvent was removed from the filtrate under reduced pressure. The resulting residue was slurried with a mixed solvent of petroleum ether (250 mL) and ethyl acetate (200 mL) at room temperature for 20 minutes, and filtered. The filter cake collected and dried under vacuum to give the target compound 7. 1H NMR (400 MHz, CDCl3) δ: 8.38 (s, 1H), 7.67 (s, 1H), 6.00 (t, J=5.8 Hz, 1H), 4.58 (t, J=4.5 Hz, 2H), 3.98 (t, J=4.5 Hz, 2H), 3.49 (t, J=5.0 Hz, 2H), 3.26 (s, 3H), 3.25-3.21 (m, 2H), 2.45 (br s, 1H).

Step 6: Synthesis of Compound 8

Compound 7 (108.02 g, 0.29 mol), 3,4-dimethylenedioxyphenylboronic acid pinacol ester (94.27 g, 0.38 mol) and cesium carbonate (283.46 g, 0.87 mol) were dissolved in a mixed solvent of dioxane (2.10 L) and water (210mL) at 5-10° C. under nitrogen protection. Then [1,1′-bis(diphenylphosphino)ferrocene]palladium dichloride (32.20 g, 0.044 mol) was added and the reaction mixture was heated to 85° C. and stirred for 15 hours. After the reaction was complete, the reaction was cooled to room temperature, and the solvent was removed under reduced pressure, and added to cold water (3.0 L). The pH was adjusted to 3-4 with dilute hydrochloric acid. Extraction was conducted with ethyl acetate (1.2 L×4). The organic phases were combined, washed with saline (1.50 L), dried over anhydrous sodium sulphate, and filtered. The solvent was removed from the filtrate under reduced pressure. The resulting residue was separated by column chromatography (eluent: dichloromethane/methanol=100/0-100/1, v/v) to give the target compound 8. MS-ESI m/z: 413.0 [M+H]+.

Step 7: Synthesis of the Compound of Formula (I)

Sodium hydride (29.89 g, 0.75 mol, purity: 60%) was added into anhydrous tetrahydrofuran (1.40 L) in batches at 5-10° C. under nitrogen protection. Then anhydrous tetrahydrofuran (500 mL) solution of compound 8 (63.05 g, 0.15 mol) was added into the reaction solution. The reaction mixture was stirred at 5-10° C. for 1 hour. Then 5-bromo-2-chloropyrimidine (44.49 g, 0.23 mol) and anhydrous N,N-dimethylformamide (63 mL) were added sequentially and the reaction mixture was heated to 70-75° C. and the reaction was stirred for another 4 hours. After the reaction was complete, the reaction mixture was cooled to room temperature, and slowly poured into a cold saturated ammonium chloride solution (6.0 L). The pH was adjusted to 3-4 with 2 M dilute hydrochloric acid. Extraction was conducted with ethyl acetate (1.5 L×4). The organic phases were combined, washed with saline (2.0 L), dried over anhydrous sodium sulphate, and filtered. The solvent was removed from the filtrate under reduced pressure. The resulting crude product was dissolved in a mixed solvent of dichloromethane (70 mL) and methanol (240 mL) and refluxed with stirring for 1 h. The heating was turned off and the mixture stirred at 5-10° C. for 12 h. The mixture was filtered and the filter cake was collected. The filter cake was dissolved with dichloromethane (200 mL). Activated carbon (20 g) was added. The mixture was stirred at room temperature for 3 h, and filtered. The solvent was removed from the filtrate under reduced pressure. The resulting residue was slurried with a mixed solvent of dichloromethane (70 mL) and methanol (240 mL) for 12 h, and filtered. The filter cake was collected, washed with methanol (20 mL) and dried under vacuum to give the compound of formula (I). MS-ESI m/z: 568.9 [M+H]+, 570.9 [M+H+2]+. 1H NMR (400 MHz, CDCl3) δ: 8.49 (s, 2H), 8.45 (s, 1H), 7.01 (s, 1H), 6.87-6.85 (m, 1H), 6.71-6.69 (m, 2H), 6.05-6.02 (m, 3H), 4.73-4.71 (m, 2H), 4.65-4.63 (m, 2H), 3.49 (t, J=5.0 Hz, 2H), 3.29 (s, 3H), 3.19-3.15 (m, 2H).

Example 2: Preparation of Crystal Form A of the Compound of Formula (I)

The compound of formula (I) (168.00 g, 0.30 mol) was added to acetonitrile (1.85 L) at 10-20° C. The mixture was heated to 75-85° C. and stirred for 2 hours until the solution became clear. The activated carbon (100.05 g) was added to the mixture, which was stirred at 75-85° C. for 3 hours. The mixture was filtered through 50.01 g of diatomite while still hot and the filtrate was stirred for 15 hours to cool naturally to room temperature of 10-20° C. (a large amount of solids precipitated). The mixture was filtered and the filter cake was washed with acetonitrile (100 mL×3). The filter cake was collected and dried under vacuum in a vacuum drying oven to give the Crystal Form A of the compound of formula (I).

About 50 mg of the compound of formula (I) was weighed and added into a 1.5 mL HPLC vial. 400 μL of tetrahydrofuran was added. Mixed well with sonication. The suspension sample was stirred on a magnetic stirrer (40° C.) under protection from light for 48 h. The solid was collected by centrifugation and then dried overnight (16-24 h) in a vacuum drying oven at 30° C. to obtain the Crystal Form A of the compound of formula (I).

About 50 mg of the compound of formula (I) was weighed and added into a 1.5 mL HPLC vial. 400 μL of acetonitrile was added. Mixed well with sonication. The suspension sample was stirred on a magnetic stirrer (40° C.) under protection from light for 48 hours. The solid was collected by centrifugation and then dried overnight (16-24 hours) in a vacuum drying oven at 30° C. to obtain the Crystal Form A of the compound of formula (I).

Example 3: Solid Stability Test for Crystal Form A of the Compound of Formula (I)

According to the Guideline for Stability Testing of APIs and Formulations (Chinese Pharmacopoeia 2015 Edition, Volume IV, General Principles 9001). The stability of Crystal Form A of the compound of formula (I) was examined under conditions of: high temperature (60° C., open), high humidity (room temperature/92.5% relative humidity, open), accelerated conditions (25° C./60% relative humidity, 40° C./75% relative humidity, sealed), and strong light (4500±500 lux, 90 μw/cm2, sealed).

1.5 g of the Crystal Form A of the compound of formula (I) was weighed and added onto an open Petri dish and spread into a thin layer. After being placed under high temperature and high humidity conditions, samples were placed in a desiccator for examination. On the 5th, 10th and 30th days, samples were taken for testing, and the results were compared with the initial test results on day 0. Samples placed under strong light condition were covered with a transparent lid and sealed with a sealing film and samples were taken on the 5th and 10th for testing and the results were compared to the initial test results on day 0. Aliquots of 2.0 g of the Crystal Form A of the compound of formula (I) was weighed. Each aliquot was placed in a double-layer LDPE bag. Each layer of LDPE bag was sealed by tying, respectively. Then the LDPE bag was placed in an aluminum foil bag and heat sealed and placed at 25° C./60% relative humidity. Samples were taken at the 3th month, 6th month, 9th month and 12th month, and placed under 40° C./75% relative humidity. Samples were taken at the 1st month, 2ed month, 3th month and 6th month, respectively. The test results were compared with the initial test results on day 0. The test results are shown in Table 4 below.

TABLE 4 Results of solid stability tests on Crystal Form A of the compound of formula (I) at high temperature, high humidity and strong light conditions Crystal Form A Sampling of the compound Total time of formula (I) impurities Test conditions points Appearance Crystal Form (%) (%) — 0 day White powder Crystal Form A 99.2% 0.26% High temperature (60° C., open) 5 days White powder — 100.1% 0.30% 10 days White powder — 100.0% 0.31% 30 days White powder — 99.1% 0.14% High humidity (room temperature/ 5 days White powder — 99.7% 0.30% 92.5% relative humidity, open) 10 days White powder — 99.5% 0.31% 30 days White powder — 99.5% 0.15% Strong light (4500 ± 500 lux-hr, 5 days White powder — 99.7% 0.29% 90 μw-hr/cm2, sealed) 10 days White powder — 99.6% 0.30% 40° C., 75% relative humidity, 1 month White powder — 99.2% 0.14% sealed 2 months White powder — 99.3% 0.14% 3 months White powder Crystal Form A 100.6% 0.13% 6 months White powder Crystal Form A 100.2% 0.20% 25° C./60% relative humidity, 3 months White powder Crystal Form A 100.2% 0.13% sealed 6 months White powder Crystal Form A 100.1% 0.20% 9 months White powder — 100.0% 0.13% 12 months White powder — 100.1% 0.16% “—”: not determined.

Conclusion: Crystal Form A of the compound of formula (I) had good stability under high temperature, high humidity or strong light condition.

Example 4: Stability Test of Crystal Form A of the Compound of Formula (I) in Different Solvents

The crude compound of formula (I) was dissolved in dichloromethane at 38-40° C., filtered while hot, concentrated under reduced pressure to dryness to obtain mixed crystals of formula (I). Saturated solutions of mixed crystals of the compound of formula (I) in THF and ACN were prepared at 50° C., respectively.

For each of Crystal Form A and Crystal Form B of the compound of formula (I), an about 5 mg sample was weighed and added to saturated solutions in different solvents at different temperatures according to the table below, and placed in a mixer at the corresponding temperature and then stirred for 3 days.

The suspension was centrifuged. The precipitate was taken and dried overnight in a vacuum oven at 30° C. The dried product was subjected to XRPD to determine the status of the crystal forms. The results are shown in Table 5.

TABLE 5 Stability tests of crystal form a in different solvents Temperature Solvent addition Status No. Solvent (° C.) (mL) (3 days later) Crystalline 1 Acetonitrile 25 0.3 Precipitation Crystal Form A 2 Acetonitrile 50 0.3 Precipitation Crystal Form A 3 Tetrahydrofuran 25 0.3 Precipitation Crystal Form A 4 Tetrahydrofuran 50 0.3 Precipitation Crystal Form A Experimental conclusion: Crystal Form A of the compound of formula (I) had good stability in acetonitrile and tetrahydrofuran at both 25° C. and 50° C.

Example 5: Study of Hygroscopicity of Crystal Form A of the Compound of Formula (I)

Experimental methods:

  • 1) Two dry stoppered glass weighing bottles (50 mm external diameter, 30 mm high) were taken and kept in a desiccator with a saturated solution of ammonium chloride in the lower part. The weighing bottles were left open. The lid of the desiccator was closed and the desiccator was placed in a constant temperature room at 25° C. overnight.
  • 2) The weighing bottles were allowed to stand overnight and weighed precisely for removal, as m1 1, m1 2, m1 3 respectively.
  • 3) A sample of an appropriate amount of Crystal Form A of the compound of formula (I) was taken and spread in a weighed weighing (the thickness of the sample was 1 mm) and weighed precisely, as m2 1, m2 2, m2 3 respectively.
  • 4) The weighing bottles were left open and kept in the desiccator with the lid in a desiccator with a saturated solution of ammonium chloride in the lower part, The lid of the desiccator was closed and then the desiccator was placed in a thermostat at 25° C. for 24 hours.
  • 5) After 24 hours, the weighing bottles were capped and then taken out of the desiccator and weighed precisely, as m3 1, m3 2, m3 3.
  • 6) The moisture-absorption weight gain was calculated as follows: Weight gain percentage=100%×(m3−m2)/(m2−m1)

The results are shown in Table 6.

TABLE 6 Samples m1 (mg) m2 (mg) m3 (mg) Weight gain percentage (%) Mean (%) Crystal Form A of the 35163.24 35703.21 35703.82 0.11 0.075 compound of formula (I) Crystal Form A of the 33118.09 33764.59 33764.82 0.04 compound of formula (I) Experimental conclusion: The moisture-absorption weight gain of Crystal Form A of the compound of formula (I) is 0.075%, which was less than 0.2%, indicating non- or almost non-hygroscopic.

Example 6: Preparation of Crystal Form B of the Compound of Formula (I)

About 120 mg of the compound of formula (I) was weighed and added into an 8 mL glass vial. 4 mL of tetrahydrofuran was added. Sonication is conducted for complete dissolution. Samples were stirred on a magnetic stirrer (40° C.). Then an equivalent amount of L-arginine was weighed, and stirred for 18 hours. The suspension was centrifuged. The solid was taken and dried under vacuum (16-18 hours, 35° C.) to obtain the Crystal Form B of the compound of formula (I).

Experimental Example 1. In Vitro Testing of the Antagonistic Effects on Human ETA Receptors Purpose of the Experiment:

The antagonistic activity of the compounds on endogenously expressed human ETA receptors in SK-N-MC cells was assessed by measuring the effects of the compounds on changes in cytoplasmic Ca2+ ion signaling induced by an agonist of human ETA receptor using a fluorescence assay. The functional activity of the ETA receptor antagonistic effect was tested at Eurofins-Cerep SA according to current standard operating procedures.

Experimental Protocol:

  • 1. Cells were suspended in Dulbecco's modified Eagle medium solution (DMEM, Invitrogen) supplemented with 1% FCSd and then distributed at a density of 5×104 cells/well in 384 plates (100 μL/well).
  • 2. Hank's Balanced Salt Solution (HBSS, Invitrogen) supplemented with 20 mM 4-(2-hydroxyethyl) piperazine-1-ethanesulfonic acid (Hepes, Invitrogen) (pH 7.4) was mixed with the fluorescent probe (Fluo4 NW, Invitrogen) and added to each well. Equilibrated with the cells for 60 minutes at 37° C. and then for 15 min at 22° C.
  • 3. The assay plate was placed in a microplate reader (CellLux, PerkinElmer). DMSO solution of the test compound and the positive control in appropriate concentration or HBSS buffer was added. After 5 minutes, 1 nM endothelin-1 or HBSS buffer (basal control) was added. Then the change in fluorescence intensity was measured. The fluorescence intensity is in proportion to the Ca2+ ion concentration of the free cytosol.
  • 4. The result was obtained as the percentage inhibition of the control response to 1 nM endothelin-1.
  • 5. The standard positive control was BQ-123 and several concentrations were tested in each experiment and the data was analyzed using Prism to produce a concentration-response curve to calculate the IC50 values of the compounds.
  • 6. The results of the experiment are shown in Table 7.

Experimental Example 2: In Vitro Testing of the Antagonistic Effect on Human ETB Receptors Purpose of the Experiment:

The antagonist activities of the compounds on human ETB receptors expressed in transfected CHO cells were assessed by measuring the effects of the compounds on changes in cytoplasmic Ca2+ ion signaling induced by an agonist of human ETB receptor using a fluorescence assay. The functional activity of the ETB receptor antagonistic effect was tested at Eurofins-Cerep SA according to current standard operating procedures.

Experimental Protocol:

  • 1. Cells were suspended in DMEM buffer (Invitrogen) and then distributed at a density of 3×104 cells/well in 384 plates (100 μL/well).
  • 2. HBSS buffer (Invitrogen) supplemented with 20 mM Hepes (Invitrogen) (pH 7.4) was mixed with the fluorescent probe (Fluo4 Direct, Invitrogen) and added to each well. Equilibrated with the cells for 60 minutes at 37° C. and then for 15 minutes at 22° C.
  • 3. The assay plate was placed in a microplate reader (CellLux, PerkinElmer). DMSO solution of the test compound and the positive control or HBSS buffer in appropriate concentration was added. After 5 minutes 0.3 nM endothelin-1 or HBSS buffer (basal control) was added. Then the change in fluorescence intensity was measured. The fluorescence intensity is in proportion to the Ca2+ ion concentration of the free cytosol.
  • 4. The result was obtained as the percentage inhibition of the control response to 0.3 nM endothelin-1.
  • 5. The standard positive control was BQ-788 and several concentrations were tested in each experiment and the data was analyzed using Prism to produce a concentration-response curve to calculate the IC50 values of the compounds.
    Note: BQ-123 is a selective ETA endothelin receptor antagonist used as a biochemical tool in endothelin receptor function studies; BQ-788 is a selective ETB endothelin receptor antagonist used as a biochemical tool in endothelin receptor function studies.

TABLE 7 In vitro antagonistic activity of Crystal Form A of the compound of formula (I) on human ETA and ETB receptors and its selectivity over ETB ETA IC50 ETB IC50 ETA/ETB Test article (nM) (μM) Selectivity Crystal Form A 1.6 32 20000 of the compound of formula (I) BQ-123 0.61/0.48 / / BQ-788 / 0.13/0.091 / Note: “/” means not measured.

Conclusion: Crystal Form A of the compound of formula (I) exhibited very high in vitro antagonistic activity against the human ETA receptor. The selectivity of Crystal Form A of the compound of formula (I) of the present disclosure for ETA over ETB was as high as 20,000-fold.

Experimental Example 3: Human Pregnane X Receptor (PXR) Test Purpose of the Experiment:

To assess the induction of PXR-mediated CYP3A expression by the compounds.

Experimental Materials and Equipment:

Name Source Type DPX2 Cell Puracyp / Dosing Media Puracyp D-500-100 P450-Glo ™ CYP3A4 Assay Promega V9001 and Screening System (Luciferin-IPA & Luciferin Detection Reagent) CellTiter-Fluor ™ Kit Promega G6081 (CTF buffer & Assay Buffer) One Glo ™ kit Promega E6110 (ONE-Glo ™ Luciferase Assay Buffer & ONE-Glo ™ Assay Substrate)

Experimental Protocol:

  • 1. The DPX2 cells was thawed under aseptic conditions.
  • 2. The DPX2 cytosol was distributed in 96-well plates (100 μl/well) and placed the plates in a 5% CO2/37° C. incubator overnight.
  • 3. The quantitative feeding medium was thawed in a 37° C. water bath. The positive control rifampicin was thawed at room temperature. A series of the test compound and positive control dilutions were prepared in quantitative feeding medium. The medium was carefully aspirated and discarded from each well, without disturbing the cells during the aspiration process. 100 μl of each concentration of the test compound was transferred to pre-labeled wells. The positive control group and the blank group were processed in the same way. The plates were placed back in the incubator and exposed for 24 hours.
  • 4. Enzyme activity test:
    • (1) 7 μl of Luciferin-IPA was added to 7 ml of quantitative feeding medium, inverted to mix, and poured into the Luciferin-IPA reagent tank.
    • (2) The 96-well plate was taken out of the incubator and the medium was carefully aspirated from each well. 50 μl of the Luciferin-IPA reagent was added to each well and the cell plate was placed back into the incubator for incubation of 60 minutes.
    • (3) During incubation, the P450-Glo buffer was poured into the Luciferin assay reagent and inverted to mix.
    • (4) The 96-well plate was taken out of the incubator. 40 μl of solution was transferred from each well to the corresponding white 96-well plate. The corresponding position of each well was kept in line with the original cell plate.
    • (5) After transferring the P450-Glo™ solution to the replicate plate, 10 ml of Cell Titration Buffer (CTF buffer) was transferred to a 15 ml sterile conical tube. 5 μl of CellTiter-Fluor™ reagent was added. Inverted to mix.
    • (6) Using a multi-channel pipette, 100 μl of CellTiter-Fluor™ reagent was gently added to the 96-well plate in which the cells were originally cultured. The plate was placed back to the incubator for 60 minutes.
    • (7) 40 μl of Luciferin detection reagent/P450-Glo buffer was added to each well of the replicate plate, stirred and incubated for 20 minutes at room temperature.
    • (8) After incubation with Luciferin detection reagent for 20 minutes, a luminometer (set for 1-5 seconds. Read out time) was used to determine the luminescence of each well of the white 96-well plate. Relatively high gain settings should be used.
    • (9) ONE-Glo™ luciferase assay buffer to ONE-Glo™ test reagent was added, inverted to mix.
    • (10) After incubation at 37° C. for 60 minutes, the original 96-well plate was taken out of the incubator, the microplate reader was set to fluorescence mode and the excitation wave length was set to 380-400 nm and the emission wave length to 505 nm. The fluorescence intensity of each well was measured.
    • (11) The cell plate was removed from the microplate reader. 100 μl of ONE-Glo™ test reagent was added to each well. The plate was shaken to mix and incubated at room temperature for 5 minutes.
    • (12) The microplate reader was set to 5 s pre-shake and 5 s well reading. The fluorescence intensity of each well was measured. A high instrument gain (sensitivity) setting should be used.
  • 5. The activation effect of the drug on PXR was reflected by fold induction, i.e. fold induction of each group=luciferase activity value of the drug-treated group/luciferase activity value of the solvent control group. This was used to predict its induction on CYP3A4. The positive control was rifampicin. Six concentrations were tested in each experiment and the data was analyzed using Prism to produce a concentration-response curve to calculate the EC50 values of the compounds.

Results:

The test results are shown in Table 8.

TABLE 8 Results of induction of PXR-mediated CYP3A expression by the compound of the present disclosure Test Compound of Control compound compound formula (I) (Macitentan) EC50 (μM) 27.6 ± 1.33* 6.34 ± 0.170* *Calculation error of the simulation curve

Conclusion:

The compound of formula (I) of the present disclosure showed a weak induction of PXR-mediated CYP3A expression while the compound Macitentan showed a strong induction of PXR-mediated CYP3A expression. Therefore, the compound of formula (I) was superior to Marcitetan in the characterization experiments of PXR-mediated induction of CYP3A expression.

Experimental Example 4: Inhibition Assay for Human Liver Microsomal Cytokine P450 Isozymes Purpose of the Experiment:

The aim of the project was to evaluate the inhibitory activity of the test article against human liver microsomal cytochrome P450 isozymes (CYP1A2, CYP2C9, CYP2C19, CYP2D6 and CYP3A4) using a 5-in-1 probe substrate for CYP isozymes.

Experimental Protocol:

Mixed human liver microsomes (HLM) were purchased from Corning Inc. (Steuben, N.Y., USA) and stored at less than −80° C. prior to use. A diluted series of concentrations of the stock solution of the test article was added to an incubation system containing human liver microsomes, probe substrate and cofactors of the circulatory system. The control without the test article but with solvent was used as the enzyme activity control (100%). The concentration of metabolites generated by the probe substrate in the samples was determined by liquid chromatography-tandem mass spectrometry (LC-MS/MS). A non-linear regression analysis of the mean percentage activity of the test article against concentration was performed using SigmaPlot (V.11). The IC50 values were calculated using a three- or four-parameter inverse hyperbolic logarithmic function.

Results:

The test results are shown in Table 9.

TABLE 9 Results of inhibition of the compound of the present disclosure on human liver microsomes cytochrome P450 isozymes P450 isozyme inhibition IC50 (μM) Compound CYP1A2 CYP2C9 CYP2C19 CYP2D6 CYP3A4-M Control compound (Macitentan) 37.4 7.5 31.7 >50 23.0 Compound of formula (I) 47 >50 >50 >50 18

Conclusion:

The compound of formula (I) of the present disclosure shows very weak inhibition on all five major isozymes of CYP, while Macitentan shows weak inhibition on four major isozymes of CYP and moderate inhibition on the isozyme CYP2C9. Therefore, the compound of formula (I) was superior to Macitentan in the characterization experiments of the inhibition of the five major isozymes of cytokine P450 in human liver microsomes.

Experimental Example 5: Inhibition Test of the Compounds on Bile Salt Export Pump (BSEP) Purpose of the Experiment:

In this experiment, the ability of the bile salt export pump (BSEP) to absorb the substrate taurocholic acid TCA was assessed by LC/MS/MS to determine whether the test compound had inhibitory effect on the bile salt export pump transport process.

Experimental Material:

Name Source BSEP-Hi5-VT Solvo Biotechnology Cat#: SB-BSEP-Hi5-VT 1.0M TRIS Buffer pH 7.4 Invitrogen Cat#: 15567-027 Sucrose Sigma Cat#: 84100 Tris Base Sigma Cat#: T1503 Taurocholic Acid Sigma Cat#: T4009 ATP (disodium salt) Sigma Cat#: A-2383 1M HEPES Gibco Cat#: 15630-080 AMP (disodium salt) Sigma Cat #: 01930 0.5M EDTA Biosolution Cat#: BIO260-15 Methanol Sigma Cat#: 494437 Multiscreen 384-well FC Millipore filter plates -1.2 micron Cat#: MZFCN0W10 glass fiber ECHO LDV plate LabCYTE Cat#: LP-0200 384-well polypropylene plate Costar Cat#: 3656 ECHO 550 LabCYTE Internal standard HDBiosciences

Solution Preparation:

  • 1. Buffer A:

50 mM HEPES pH 7.4, 100 mM KNO3, 10 mM Mg(NO3)2, 50 mM Sucrose.

  • 2. Buffer B:

10 mM TRIS pH 7.4, 100 mM KNO3, 10 mM Mg(NO3)2, 50 mM Sucrose.

  • 3. ATP Buffer:

Prepared using Buffer A. 12 ml of Buffer A containing 8.16 mM ATP, 4.08 μM Taurocholic acid.

  • 4. AMP Buffer:

Prepared using Buffer A. 12 ml of Buffer A containing 8.16 mM AMP, 4.08 μM Taurocholic acid.

  • 5. BSEP-Hi5-VT Vesicle solution:

Prepare a solution containing 5 μg/μL of BSEP-Hi5-VT using Buffer A.

Sample Preparation:

  • 1. Compounds were diluted to 100 mM with DMSO; then subjected to a serial dilution of 3-fold for eleven dilutions. The minimum concentration was 0.169 μM.
  • 2. 20 mM DMSO solution of the positive reference Glyburide (Glibenclamide) was prepared; then subjected to a serial dilution of 2-fold for eleven dilutions. The minimum concentration was 19.5 μM.

Experimental Protocol:

  • 1. ECHO was used to transfer 0.3 μl of DMSO solution of the compounds or diluted DMSO to the corresponding wells of the compounds plate, respectively.
  • 2. 14.7 μl of ATP Buffer was added into the corresponding wells of the compounds and the zero percent effect (ZPE), respectively.
  • 3. 14.7 μl of AMP Buffer was added into the corresponding wells of the hundred percent effect (HPE).
  • 4. The plate was shaken for 10 minutes at 25° C.
  • 5. 15 μl of BSEP-Hi5-VT Vesicle solution was added to each well separately and the plate was shaken for a further 40 minutes at 25° C.
  • 6. 5 μl of 0.5 M Ethylenediaminetetraacetic acid (EDTA) solution was immediately added to each well, followed by 65 μl of Buffer B. All reactions were complete.
  • 7. After the reactions were complete, 95 μl of liquid was transferred from the compounds plate to the filter plate using apparatus.
  • 8. The liquid receiving plate was placed under the filter plate. Then the liquid was removed using a centrifuge. The liquid on the receiving plate was discarded.
  • 9. 90 μl of Buffer B was added to the filter plate. The liquid receiving plate was placed under the filter plate. Then the liquid was removed using a centrifuge. The liquid on the receiving plate was discarded. The filter plate was washed three times in total.
  • 10. The filter plate was left to dry overnight.
  • 11. On the next day, 80 μl of methanol/water (80/20, v/v) solution was added to the filter plate.
  • 12. The plate was vibrated for 15 minutes after applying the film to the filter plate.
  • 13. A new liquid receiving plate was placed under the filter plate and centrifugation was conducted for 5 minutes to filter all the liquid from the filter plate into the receiving plate.
  • 14. 15 μl of internal standard solutions was added to each well of the liquid receiving plate and the plate was sealed with sealing film.
  • 15. Taurocholic acid in the receiving plate was determined using LC/MS/MS.

Several concentrations were tested in each experiment and the data was analyzed using Prism to produce a concentration-response curve to calculate the IC50 values of the compounds.

Results:

The results of the test are shown in Table 10.

TABLE 10 Results of the inhibition of the compound of the present disclosure on Bile salt export pump (BSEP) Compound of Compound Glibenclamide Macitentan formula (I) IC50 (μM) 1.489 0.47 43.77

Conclusion:

The compound of formula (I) of the present disclosure exhibits extremely weak inhibitory effect on bile salt export pump (BSEP), On the contrary, Macitentan exhibits strong inhibitory effect. Therefore, the compound of the present disclosure has much weaker inhibitory effect on bile salt export pump than Macitentan, thereby significantly reducing the risk of producing hepatotoxicity.

Experimental Example 6: Pharmacokinetic Evaluation of the Compounds in Rats Purpose of the Experiment:

The animals used in this study were SD male rats. The LC/MS/MS method was applied to quantify the plasma drug concentrations in rats at different time points after administration of the test compound intravenously or orally by gavage in order to evaluate the pharmacokinetic characteristics of the test compound in rats.

Experimental Material:

Sprague Dawley (SD) rats (male, 200-300 g, 7-10 weeks old, Beijing Vital River or Shanghai SLAC).

Experimental Operations:

A clear solution of the test compound was administered to SD rats by tail vein injection (overnight fasting) or oral gavage (overnight fasting). At 0 hour (before administration through tail vein injection) and 0.0833, 0.25, 0.5, 1, 2, 4, 6, 8 and 24 hours after administration through tail vein injection, 200 μL of blood was collected by jugular venipuncture into anticoagulation tubes supplemented with EDTA-K2 (Jiangsu Kangjian Medical Supplies Co., Ltd.). The mixture in the anticoagulation tube was vortexed thoroughly at 4° C. and then centrifuged at 13,000 rpm for 10 minutes to obtain the plasma. At 0 hours (before administration by oral gavage) and 0.5, 1, 2, 4, 6, 8 and 24 hours after administration by oral gavage, 200 μL of blood was collected by jugular venipuncture into anticoagulation tubes supplemented with EDTA-K2 (Jiangsu Kangjian Medical Supplies Co., Ltd.). The mixture in the anticoagulation tube was vortexed thoroughly and the plasma was then centrifuged at 13,000 rpm for 10 minutes to obtain the plasma. Blood concentrations were determined by LC/MS/MS and the relevant pharmacokinetic parameters were calculated using WinNonlin™ Version 6.3 (Pharsight, Mountain View, Calif.) pharmacokinetics software with a non-compartmental model linear-log trapezoidal method.

Results:

The results of the test are shown in Table 11.

TABLE 11 Pharmacokinetic parameters of the compound of the present disclosure in rats Intravenous injection (2 mg/kg) Oral (10 mg/kg) Area under Area under the drug the drug Pharmacokinetic Plasma Half- concentration- Peak Peak concentration- parameters clearance life time curve concentration time time curve Bioavailability in rats (mL/min/kg) (h) (μM · h) (μM) (h) (μM · h) (%) Compound of 3.71 1.14 16.09 31.99 0.25 60.22 74.9 formula (I)

Conclusion:

The compound of formula (I) had low plasma clearance (<5 mL/min/kg) and high oral gavage bioavailability (>70%) in rats.

Experimental Example 7: Pharmacokinetic Evaluation of the Compounds in Beagle Dogs Purpose of the Experiment:

Male Beagle dogs were used as the test animals in this study. The LC/MS/MS method was applied to quantify the plasma drug concentrations in Beagle dogs at different time points after administration of the test compound by intravenous injection or oral gavage to evaluate the pharmacokinetic profile of the test compound in Beagle dogs.

Experimental Material:

Beagle dogs (Male, 6-15 kg, above 6 months, Beijing Marshall Biotechnology Co.)

Experimental Operations:

A clear solution of the test compound was administered to the Beagle dogs by intravenous injection (overnight fasting) or oral gavage (overnight fasting). At 0 h (before administration by intravenous injection) and at 0.0833, 0.25, 0.5, 1, 2, 4, 6, 8 and 24 h after administration by intravenous injection, about 500 μL of blood was collected from peripheral blood vessels into anticoagulation tubes supplemented with EDTA-K2 (Jiangsu Kangjian Medical Supplies Co., Ltd.). At 0 hours (before administration by oral gavage) and 0.25, 0.5, 1, 2, 4, 6, 8 and 24 hours after administration by oral gavage, about 500 μL of blood was collected from peripheral blood vessels into anticoagulation tubes supplemented with EDTA-K2. The mixture in the anticoagulation tube was vortexed thoroughly at 4° C. and the plasma was then centrifuged at 13,000 rpm for 10 minutes to obtain the plasma. Blood concentrations were determined by LC/MS/MS and the relevant pharmacokinetic parameters were calculated using WinNonlin™ Version 6.3 (Pharsight, Mountain View, Calif.) pharmacokinetics software with a non-compartmental model linear-log trapezoidal method.

Results:

The results of the test are shown in Table 12.

TABLE 12 Pharmacokinetic parameters according to the compound of the present disclosure in Beagle dogs Intravenous injection (1 mg/kg) Oral (3 mg/kg) Area under Area under the drug the drug Pharmacokinetic Plasma Half- concentration- Peak Peak concentration- parameters clearance life time curve concentration time time curve Bioavailability in rats (mL/min/kg) (h) (μM · h) (μM) (h) (μM · h) F (%) Compound of 4.79 0.86 7.56 12.75 0.38 33.40 147 formula (I)

Conclusion:

The compound of formula (I) of the present disclosure had low plasma clearance (<5 mL/min/kg) and high oral gavage bioavailability (>50%) in Beagle dogs.

Experimental Example 8: In Vivo Pharmacodynamic Evaluation of the Compounds Purpose of the Experiment

The animal model of pulmonary hypertension in SD rats induced by monocrotaline (MCT) was used in this study to examine the pharmacological effects of the test compound on a rat model of pulmonary hypertension.

Experimental Material: Experimental Animals

Species: Rat

Strain: Sprague-Dawley

Age at arrival at animal house: 5 weeks

Gender: Male

Animal weight at the start of the experiment: 200-260 g

Number: 88 (81 for pharmacodynamic (PD) and pharmacokinetic (PK) tests and 7 for PK-blank matrix)

Supplier: Shanghai SLAC Experimental Animals Co.

Certificate of the animals: 20170005008695

Other Reagent Information

TABLE 13 Reagent information sheet Name Manufacturers Batch number Storage conditions MCT Sigma-Aldrich WXBC5062V 2-8° C. Tween 80 Sigma-Aldrich BCBV8843 room temperature PEG400 Sigma-Aldrich BCBZ7335 room temperature 4% Dingguo 92H001335 4° C. Paraformaldehyde changsheng fixative biotech CO. LTD

Preparation of Key Reagents and Solutions of the Compounds:

20 mg/mL MCT solution: an appropriate amount of MCT was weighed and added to a flask with an appropriate volume. Firstly, MCT was fully dissolved with a small amount of 1 mol/L HCl, then pH was adjusted to 7-7.5 with 10 mol/L NaOH, and finally physiological saline was added to achieve the total volume.

Solvent: 20% PEG 400+0.5% Tween 80 dissolved in deionized water. The pH was adjusted to 9±0.1.

Solutions of 3 mg/mL Macitentan, 0.1 mg/mL, 0.3 mg/mL and 1 mg/mL the compound of formula (I): an appropriate amount of the compound was weighed and added to a flask with an appropriate volume. PEG 400 of 20% of the total volume was added. Heating and stirring were conducted at 40° C. Tween 80 of 0.5% of the total volume was added. Heating and stirring were conducted at 40° C. Deionized water of 70-75% of the volume was added. Heating and stirring were conducted at 40° C. The pH was adjusted with 5 N NaOH until became clear. Then the pH was reversely adjusted to less than 9 with 6 N HCl and 1 N HCl. The remaining volume was made up with deionized water to achieve the total volume. The final pH was determined (9±0.1).

30 mg/mL sodium pentobarbital solution: an appropriate volume of sodium pentobarbital stock solution was measured and added into a flask with an appropriate volume and diluted to final concentration with physiological saline.

Instrument Information:

TABLE 14 Instrument information sheet Name Manufacturers Type Multi-channel physiological Chengdu Instrument RM6240C signal acquisition and processing Factory system Small animal ultrasound imaging VISUALSONICS Vevo1100 Centrifugal machine Eppendorf centrifuge 5417R

Grouping of Animals

After the animals had been acclimatized for about 1 week, the animals were randomized into 9 groups according to body weight and the condition of the animal, as shown in Table 15.

TABLE 15 Experimental animal grouping and dosing regimen Induction Administration Days of Test Group Number of (subcutaneous/ Medication/ concentration administration classification Group No. animals single dose) route/frequency (mg/mL) (Day) PDTEST Blank group G1 12 NS Vehicle/gavage — 21 consecutive administration/ days of once a day administration Vehicle group G2 12 MCT Vehicle/gavage — 21 consecutive administration/ days of once a day administration Macitentan G3 12 MCT Macitentan/gavage 3 21 consecutive −30 mg/kg administration/ days of once a day administration Compound of G4 12 MCT Compound of 0.1 21 consecutive formula (I) formula (I)/ days of −1 mg/kg PO/QD administration Compound of G5 12 MCT Compound of 0.3 21 consecutive formula (I) formula (I)/ days of −3 mg/kg PO/QD administration Compound of G6 12 MCT Compound of 1 21 consecutive formula (I) formula (I)/ days of −10 mg/kg PO/QD administration PKTEST PK-Mac G7 3 MCT Macitentan/ 3 21 consecutive −30 mg/kg PO/QD days of administration PK- G8 3 MCT Compound of 0.1 21 consecutive Compound of formula (I)/ days of formula (I) PO/QD administration −1 mg/kg PK- G9 3 MCT Compound of 0.3 21 consecutive Compound of formula (I)/ days of formula (I) PO/QD administration −3 mg/kg Note: Mac represents Macitentan.

Monitoring Indicators Monitoring Indicators in PD Tests

1) Daily monitoring of the general condition of the animals and their body weights;

2) Right ventricular function tests: right ventricular ejection fraction (RVEF), right ventricular wall thickness (RVWT);

3) Hemodynamic tests: right ventricular systolic pressure (RVSP);

4) Determination of the right ventricular hypertrophy index (RVHI): RV/(LV+SEP);

5) 4-HE staining to observe PAWT/IHC staining to observe PCNA as the endpoint detection.

Monitoring Indicators in PK Tests

1) Daily monitoring of the general condition of the animals and their body weights;

2) Plasma: determination of the pharmacokinetic parameters of the compounds in plasma.

Test Method B-Mode Ultrasonic Detection of RVEF, RVWT

Rats were anesthetized with 30 mg/mL pentobarbital sodium (2 mL/kg, ip) and RVEF, RVWT were measured using a small animal ultrasound instrument (VEVO-1100).

Measurement of RVSP in Rats by Right Heart Catheterization

Rats were anesthetized with 30 mg/mL sodium pentobarbital (2 mL/kg, ip), fixed onto a surgical plate in supine position, and shaved on the neck. A skin incision was made on the neck. The subcutaneous tissue and muscle layer were bluntly dissected. And the left carotid artery and right jugular vein were stripped. A rat-specific right heart catheter (a PE tube with an external diameter of about 1.5 mm and a small arc-shaped curve at the distal end) connected to a pressure transducer and filled with 0.3% heparin sodium solution was inserted into the right external jugular vein. The arc of the pulmonary artery catheter was kept downwards during the operation and the pulmonary artery catheter was threaded towards the right atrium. The pressure waveform was used to judge whether it had reached the heart. The catheter was deflected towards the left and pushed forward into the right ventricle.

Measurement of RVHI

The heart was removed. The atria and great vessels were removed. Blotted to dryness with filter paper. The right ventricle was stripped and weighed to calculate RVHI=RV/(LV+SEP).

4-HE staining to observe PAWT/IHC staining to observe PCNA as the endpoint detection

After euthanasia of the rats, the middle lobe of the right lung was removed, perfused using saline and placed in 4% paraformaldehyde for fixation for the purpose of pathological examination.

Blood Collection and Plasma Preparation

Blood samples were taken before and after dosing on the day of the endpoint, at time points of 0, 0.25, 0.5, 1, 2, 4, 6 and 8 h. The rats were placed in a fixator, 250 μL of blood was collected from the tail vein, transferred to an EP tube with anticoagulant (5-8 μL of 15% EDTA), inverted and shaken, and immediately placed on wet ice for temporary storage. The collected blood samples were placed in centrifugal machines and centrifuged at 4° C., 3000 rpm for 15 min. The plasma was collected after centrifugation and immediately placed on dry ice. After all samples have been collected and transferred to cryopreservation at −80° C. for pharmacokinetic analysis.

Statistical Analysis:

All data was entered into an Excel document and expressed as mean (Mean)±standard error of mean (SEM). One-way ANOVA with Dunnett's t test was used to analyze and compare the data of each group. Differences between two groups were compared using the unpaired two-tailed t-test method. Statistical analysis results P<0.05 were considered significantly different.

Test Results:

TABLE 16 Efficacy of the test compound in rats with pulmonary hypertension (Mean ± SEM, n = 12) 21-day Right Right Right Percentage of weight ventricular Right ventricular ventricular PCNA middle pulmonary change systolic ventricular wall ejection positivity artery intima- rate pressure hypertrophy thickness fraction rate media thickness Groups (%) (mmHg) index (mm) (%) (%) (%) Blank group 54.31 ± 2.49 20.56 ± 0.66  0.26 ± 0.01   1.01 ± 0.04  78.58 ± 1.65  2.10 ± 0.40   28.98 ± 0.71   Vehicle group   39.30 ± 1.77***  53.91 ± 3.66*** 0.48 ± 0.03***  1.39 ± 0.08***  50.45 ± 2.16*** 6.49 ± 0.86*** 50.99 ± 1.16*** Mac 45.75 ± 2.14 38.71 ± 3.52## 0.36 ± 0.03### 1.13 ± 0.04## 58.87 ± 1.71# 4.43 ± 0.42   46.56 ± 1.07#  −30 mg/kg Compound of 43.33 ± 1.56 40.72 ± 3.38#  0.40 ± 0.01#  1.16 ± 0.05#  58.48 ± 2.11# 3.6 ± 0.69## 40.44 ± 1.13### formula (I) −1 mg/kg Compound of 41.23 ± 3.47 36.70 ± 3.81## 0.38 ± 0.03##  1.11 ± 0.05##   58 ± 1.80# 3.56 ± 0.66##  35.44 ± 1.55### formula (I) −3 mg/kg Compound of 42.04 ± 3.07 37.82 ± 3.10## 0.36 ± 0.02### 1.10 ± 0.05##  59.86 ± 2.29## 2.85 ± 0.65### 40.11 ± 1.07### formula (I) −10 mg/kg ***P< 0.001, Vehicle vs Sham, t-test; #P < 0.05, ##P < 0.01, ###P < 0.001 each treatment group vs Vehicle, one-way ANOVA. Weight change rate (%) Positive values were percentage weight gain and negative values were percentage weight loss. Mac is Macitentan.

Studies of Pharmacokinetics Accompanying the Efficacy of Formula (I) and Macitentan:

Blood samples were collected before and after dosing on day 21 and collected at time points 0, 0.25, 0.5, 1, 2, 4, 6 and 8 h for analysis of plasma drug concentrations of the compound of formula (I) and Macitentan. The results showed that after administration by gavage at doses of 1 mg/kg and 3 mg/kg, respectively, the area under the drug concentration-time curve (AUC0-inf) of the compound of formula (I) in plasma was respectively 1410 and 5230 ng/mL·h, showing good dose-dependency.

TABLE 17 Pharmacokinetic parameters accompanying the efficacy of the compound of formula (I) and Macitentan in an MCT-induced rat model of pulmonary hypertension (n = 3) Compound of formula (I) Compound of formula (I) Macitentan administered by gavage administered by gavage administered by gavage 1 mg/kg 3 mg/kg 30 mg/kg Coefficient Coefficient Coefficient Pharmacokinetic Standard of variation Standard of variation Standard of variation parameters Mean deviation (%) Mean deviation (%) Mean deviation (%) Cmax (nM) 345 22.5 6.52 1120 252 22.5 1840 687 37.3 Tmax (h) 1.00 0.00 0.00 1.00 0.00 0.00 4.08 3.88 95.1 T1/2 (h) 2.30 0.343 14.9 3.64 0.368 10.1 ND — — Tlast (h) 8.00 — — 8.00 — — 8.00 — — AUC0-last 1270 45.8 3.61 4220 771 18.3 11000 5980 54.4 (ng/mL · h) AUC0-inf 1410 75.7 5.37 5540 730 13.2 ND — — (ng/mL · h) MRT0-last (h) 2.83 0.121 4.28 3.04 0.236 7.76 4.38 0.382 8.72 MRT0-inf (h) 3.64 0.154 4.23 5.52 0.765 13.9 ND — — AUC0-inf/ 111 2.52 2.27 132 8.89 6.73 ND — — AUC0-last (%)

Conclusion:

The results of the study showed that the compound of formula (I) significantly improved the indicators of pulmonary hypertension and right ventricular function in a pulmonary hypertension model: at doses of 1, 3 and 10 mg/kg it significantly reduced right ventricular systolic pressure, improved right ventricular function and inhibited proliferation of pulmonary artery smooth muscle. The compound of formula (I) was effective at 1 mg/kg and its effects at lower doses was comparable to Macitentan at 30 mg/kg.

Claims

1. A crystal form of the compound as shown in formula (I),

which is selected from the group consisting of:
(1) Crystal Form A, wherein the Crystal Form A has an X-ray powder diffraction pattern having characteristic diffraction peaks at the following 2θ angles: 12.62±0.20°, 16.86±0.20°, 19.33±0.20°, and 25.38±0.20°; and
(2) Crystal Form B, wherein the Crystal Form B has an X-ray powder diffraction pattern having characteristic diffraction peaks at the following 2θ angles: 7.51±0.20°, 9.60±0.20°, and 22.56±0.20°.

2. The Crystal Form A according to claim 1, wherein

the Crystal Form A has an X-ray powder diffraction pattern having characteristic diffraction peaks at the following 2θ angles: 8.42±0.20°, 10.31±0.20°, 12.62±0.20°, 16.86±0.20°, 18.28±0.20°, 19.33±0.2°, 21.87±0.20°, 25.38±0.20°, and 27.14±0.20°.

3. The Crystal Form A according to claim 2, wherein

the Crystal Form A has an X-ray powder diffraction pattern having characteristic diffraction peaks at the following 2θ angles: 8.42°, 9.41°, 9.58°, 9.82°, 10.31°, 12.62°, 15.77°, 16.62°, 16.86°, 17.51°, 17.97°, 18.28°, 18.85°, 19.33°, 19.58°, 20.33°, 21.87°, 22.58°, 22.93°, 23.15°, 23.39°, 25.05°, 25.38°, 26.31°, 26.63°, 27.14°, 27.79°, 29.40°, 31.01°, 31.48°, 35.42°, and 39.21°.

4. The Crystal Form A according to claim 2, wherein

the Crystal Form A has an XRPD pattern as shown in FIG. 1.

5. The Crystal Form A according to claim 1, wherein

the Crystal Form A has a differential scanning calorimetry curve having the onset point of an endothermic peak at 161.3±3.0° C.

6. (canceled)

7. The Crystal Form A according to claim 1, wherein

the Crystal Form A has a thermogravimetric analysis curve having a weight loss of 0.01% at 152.3±3.0° C.

8. (canceled)

9. (canceled)

10. The Crystal Form B according to claim 1, wherein

the Crystal Form B has an X-ray powder diffraction pattern having characteristic diffraction peaks at the following 2θ angles: 7.51±0.20°, 9.60±0.20°, 15.05±0.20°, 19.09±0.20°, 22.56±0.20°, 24.18±0.20°, 24.79±0.20°, and 27.95±0.20°.

11. The Crystal Form B according to claim 10, wherein

the Crystal Form B has an X-ray powder diffraction pattern having characteristic diffraction peaks at the following 2θ angles: 7.51°, 9.60°, 11.08°, 15.05°, 15.52°, 17.53°, 18.34°, 19.09°, 20.41°, 20.85°, 22.20°, 22.56°, 23.15°, 24.18°, 24.79°, 27.69°, 27.95°, 28.75°, 33.57°, and 35.42°.

12. The Crystal Form B according to claim 11, wherein

the Crystal Form B has an XRPD pattern as shown in FIG. 4.

13. The Crystal Form B according to claim 1, wherein

the Crystal Form B has a differential scanning calorimetry curve having the onset point of an endothermic peak at 150.3±3.0° C.

14. (canceled)

15. The Crystal Form B according to claim 1, wherein

the Crystal Form B has a thermogravimetric analysis curve having a weight loss of 0.53% 90.0±3.0° C., and a further weight loss of 0.60% at 143.9±3.0° C.

16. (canceled)

17. A process for preparing the Crystal Form A of the compound as shown in formula (I) as defined in claim 1, comprising:

(1) adding the compound as shown in formula (I) into a solvent to obtain a solution, with heating for dissolving;
(2) cooling the solution in step (1) until a solid is precipitated; stirring; and filtering to give the Crystal Form A of the compound of formula (I).

18. The process according to claim 17, wherein

the solvent is selected from the group consisting of tetrahydrofuran and acetonitrile.

19. The process according to claim 17, wherein

the stirring is conducted at the temperature of 10° C. to 60° C.

20. The process according to claim 17, wherein

the stirring time is 12 hours to 24 hours.

21. The process according to claim 17, wherein

the weight-volume ratio of the compound to the solvent is 1 g:1-6 mL.

22. A process for preparing the Crystal Form B of the compound as shown in formula (I) as defined in claim 1, comprising:

(1) adding the compound as shown in formula (I) into a solvent with complete dissolution;
(2) adding an amino acid; stirring at 40° C. for 12-24 hours; and filtering to give the Crystal Form B of the compound of formula (I);
wherein,
the solvent is selected from the group consisting of tetrahydrofuran;
the amino acid is selected from the group consisting of L-arginine.

23. A method for treating a disease related to ETA receptor antagonist, comprising administering to a subject in need thereof an effective amount of the crystal form according to claim 1.

24. The method according to claim 23, wherein,

the disease related to ETA receptor antagonist is pulmonary hypertension, essential hypertension, refractory hypertension, diabetic nephropathy or intracranial vasospasm.

25. A pharmaceutical composition comprising a crystal form according to claim 1.

Patent History
Publication number: 20220220098
Type: Application
Filed: May 22, 2020
Publication Date: Jul 14, 2022
Inventors: Junmiao LI (Shanghai), Maoyi LEI (Shanghai), Yunfu LUO (Shanghai)
Application Number: 17/595,651
Classifications
International Classification: C07D 405/14 (20060101); A61P 9/12 (20060101);